Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_assertion description "[Furthermore, the associations of APOE and TREM2 with AD were highly significant, even in gene-based rare allele analysis, which implies that further deep sequencing of these genes is required in AD heritability studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_assertion evidence source_evidence_literature NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_assertion SIO_000772 25329708 NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_assertion wasDerivedFrom befree-2016 NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_assertion wasGeneratedBy ECO_0000203 NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1230729.RAshAxSvLPSFtVosePbiyfknimiCiQcrmpQWn0MMLm5c8130_provenance.